Any hereditary pulmonary alveolar proteinosis in which the cause of the disease is a mutation in the CSF2RB gene.
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surfactant metabolism dysfunction, pulmonary, 1
MONDO:0009929
surfactant metabolism dysfunction, pulmonary, 4
MONDO:0010424
interstitial lung disease due to ABCA3 deficiency
MONDO:0012582
severe early-onset pulmonary alveolar proteinosis due to MARS deficiency
MONDO:0014206
chronic respiratory distress with surfactant metabolism deficiency
MONDO:0016323
SFTPC-related interstitial lung disease
MONDO:0018603